Cardionostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Cardionostics, Inc. makes
Cardionostics, Inc. manufactures Holter recorders, including the Holter Dura-Lite Recorder (cassette), Holter Cura-Lite Recorder, and related devices such as CardioVista, which are used for ambulatory electrocardiographic monitoring.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Cardiovista Ref K902486
Regimes: 510(k) Registry: 510(k)Cardionostics Holter Dura-Lite Recorde Ref K842954
Regimes: 510(k) Registry: 510(k)Holter Cura-Lite Recorder Ref K844977
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardionostics, Inc. have in the registry?
The registry currently lists 4 devices for Cardionostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardionostics, Inc.'s devices?
Among its 4 most recently registered devices, Cardionostics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cardionostics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cardionostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardionostics, Inc. in the registry?
The most recently registered devices listed for Cardionostics, Inc. include CARDIONOSTICS HOLTER DURA-LITE RECORDER (CASSETTE), CARDIOVISTA, CARDIONOSTICS HOLTER DURA-LITE RECORDE and HOLTER CURA-LITE RECORDER.